Company ยท US
Ascep, Inc.
FDA 510(k) clearances and medical device recalls filed under this name, 1979 to 1983. Name variants (Inc, Corp, punctuation) are merged.
9510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Apr 12, 1983 | K830219 | VARIOUS INSTRUMENTS & INSTRUMENT TRAYS Ascep, Inc. | FSM |
| Oct 22, 1982 | K822893 | G.E.V. DISPOSABLE SCALPELS Ascep, Inc. | GDX |
| Jan 26, 1981 | K810004 | STERILE DISPOSABLE INSTRUMENT TRAYS Ascep, Inc. | FSM |
| Nov 19, 1980 | K802726 | INSTRUMENTS NONSTERILE & STERILE Ascep, Inc. | HAO |
| Oct 26, 1979 | K791886 | I.V. CARE KIT Ascep, Inc. | KGX |
| Oct 22, 1979 | K791885 | I.V. START SET Ascep, Inc. | KGX |
| Oct 17, 1979 | K791889 | SUTURE REMOVAL TRAY, REORDER 7950&7951 Ascep, Inc. | FSM |
| Oct 17, 1979 | K791888 | CATHETER CARE KIT REORDER 7940&7941 Ascep, Inc. | EFQ |
| Oct 17, 1979 | K791887 | CENTRAL VENOUS CATHETER DRESSING TRAY Ascep, Inc. | FSM |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||